ENST00000285021.12:c.2241G=
MANE Select
|
ENSP00000285021.8:p.Val747=
|
|
ENST00000285021.11:c.2241G=
|
ENSP00000285021.7:p.Val747=
|
|
ENST00000427795.2:n.106G=
|
|
|
ENST00000476581.6:c.*1694G=
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ENSP00000424548.1:n.*1694G=
|
|
NM_004628.4:c.2241G= , LRG_472t1:c.2241G=
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NP_004619.3:p.Val747=
|
|
NR_027299.1:n.2221G=
|
|
|
XM_011534092.1:c.2241G=
|
XP_011532394.1:p.Val747=
|
|
NM_001354726.1:c.1662G=
|
NP_001341655.1:p.Val554=
|
|
NM_001354727.1:c.2235G=
|
NP_001341656.1:p.Val745=
|
|
NM_001354729.1:c.2223G=
|
NP_001341658.1:p.Val741=
|
|
NM_001354730.1:c.1995G=
|
NP_001341659.1:p.Val665=
|
|
NR_148950.1:n.2184G=
|
|
|
NR_148951.1:n.2060G=
|
|
|
XR_001740256.2:n.2274G=
|
|
|
XR_002959580.1:n.2274G=
|
|
|
XR_002959581.1:n.3891G=
|
|
|
NM_001354727.2:c.2235G=
|
NP_001341656.1:p.Val745=
|
|
NM_004628.5:c.2241G=
MANE Select
|
NP_004619.3:p.Val747=
|
|
NR_148950.2:n.2113G=
|
|
|
NR_148951.2:n.1989G=
|
|
|
NM_001354726.2:c.1662G=
|
NP_001341655.1:p.Val554=
|
|
NM_001354729.2:c.2223G=
|
NP_001341658.1:p.Val741=
|
|
NM_001354730.2:c.1995G=
|
NP_001341659.1:p.Val665=
|
|